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CHMP Issues Negative Opinion for Renewal of Conditional Marketing Authorization for Translarna™ (ataluren) Following Re-examination Procedure

SOUTH PLAINFIELD, N.J., Jan. 25, 2024 /PRNewswire/ -- PTC Therapeutics, Inc. announced today that the Committee for Medicinal Products for Human Use of the European Medicines Agency issued a...
United States Jeanine Clemente Kylie Okeefe Matthewb Klein Committee For Medicinal Products Human Use Therapeutics Inc

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Preventing original pharmaceuticals' price decreases in Turkey with partial preliminary injunctions

Selin Sinem Erciyas, Zeynep Çağla Üstün, and Beste Turan of Gün and Partners explain a decision by the Turkish Civil Court for Intellectual and Industrial Property Rights that set an important precedent for the protection of pharmaceutical patent holders’ rights
Civil Court Patent Office Security Institution Industrial Property Rights The Court Regulation On Implementing The Convention Ankara Court

U.S. FDA Approves Takeda's HYQVIA® as Maintenance Therapy in Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) -January 16, 2024 at 08:10 am EST

HYQVIA [Immune Globulin Infusion 10% with Recombinant Human Hyaluronidase], the Only up to Once Monthly Subcutaneous Immunoglobulin Infusion to Treat CIDP, Can Be Administered by a Healthcare...
United States Elisa Butler Van Doorn Demyelinating Polyneuropathy Giles Platford Foundation International

Eisai: The Scientific Advisory Group (SAG) to Convene to Discuss the Marketing Authorization Application for lecanemab in the EU -January 11, 2024 at 03:03 am EST

- Eisai Co., Ltd. announced today that the Scientific Advisory Group will convene to discuss the marketing authorization application of lecanemab , which is currently under review by the European...
South Korea United Kingdom Great Britain European Commission Alzheimer Clinical Trial Consortium National Medical Products Administration

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